Medical DeviceJul 5, 2023
Remel Haemophilus Test Medium (Agar) (150mm), 10/pk, REF R04033 recall — FDA Z-2038-2023
The test medium may not perform as intended.
Class IIFDA: OngoingRemel, Inc.
Latest records
Latest recalls — page 542
The newest recall records with useful source details are listed here.
Medical DeviceJul 5, 2023
Permobil PushTracker E2 component utilized with the SmartDrive MX2+ Power Assist Device recall — FDA Z-2004-2023
When multiple processes are running on the watch's Central Processing Unit (CPU), the application may fail unexpectedly. If this happens, the motor on the power assist device continues to…
Class IIFDA: OngoingPermobil
Medical DeviceJul 5, 2023
Randox Laboratories Immunoassay Premium Level 3-In vitro diagnostic use, as assayed quality recall — FDA Z-2021-2023
Delay in reporting results due to Quality Controls running high outside of range. Target value and range for ACTH in Immunoassay Premium Level 3, IA2640, lot 2031EC and Immunoassay Premium…
Class IIIFDA: OngoingRandox Laboratories Ltd.
Medical DeviceJul 5, 2023
Ellex Medical Pty Integre Pro Yellow LP561, Integre Pro Yellow LP6RY, Integre Pro Scan Green recall — FDA Z-1971-2023
When using a Laser-Indirect-Ophthalmoscope (LIO) as the delivery device, a scattered laser beam inside the laser cavity system may unintentionally exit through the Slit Lamp output port…
Class IIFDA: OngoingEllex Medical Pty Ltd.
FoodJul 5, 2023
MOTTS LLP Mott s no sugar added applesauce 6 pack 3.9 oz recall — FDA F-1016-2023
Elevated patulin levels
Class IIFDA: TerminatedMOTTS LLP
FoodJul 5, 2023
Compass USA Fresh To You Chicken Filet Sandwich recall — FDA F-1010-2023
Chicken sandwich was made with uncooked chicken.
Class IIFDA: TerminatedCompass USA
FoodJul 5, 2023
Richin Trading Sun Wave Brand Jelly Cup recall — FDA F-1299-2023
Potential choking hazard
Class IFDA: TerminatedRichin Trading Inc.
FoodJul 5, 2023
Richin Trading Sun Wave Brand Jelly Cup recall — FDA F-1300-2023
Potential choking hazard
Class IFDA: TerminatedRichin Trading Inc.
FoodJul 5, 2023
FoodJul 5, 2023
Rudolph Foods Company Rudolphs OnYums Onion Flavored Snack Rings 3 oz recall — FDA F-1012-2023
Undeclared wheat and artificial colors (Yellow 6, Yellow Lake 6, Blue 2 Lake, Blue 1 Lake, Red 40 Lake)
Class IIFDA: TerminatedRudolph Foods Company
FoodJul 5, 2023
Richin Trading Sun Wave Brand Jelly Cup recall — FDA F-1301-2023
Potential choking hazard
Class IFDA: TerminatedRichin Trading Inc.
DrugJul 5, 2023
The Harvard Drug Group Tramadol Hydrochloride Tablets, USP 50 mg, Unit Dose 100-Count recall — FDA D-0878-2023
Packaging defect: blister packaging inadequately sealed.
Class IIFDA: TerminatedThe Harvard Drug Group
VehicleJun 29, 2023
Honda master cylinder recall — NHTSA campaign 23V458000
Honda (American Honda Motor Co.) is recalling certain 2020-2021 Civic, 2020-2023 Ridgeline, 2021-2023 Passport, 2021-2022 Pilot, and 2020 Acura MDX vehicles. The tie rod fastener that…
master cylinderHonda (American Honda Motor Co.)
Medical DeviceJun 28, 2023
CRHF CRT-D DTBA2D4 VIVA XT IS1/DF4 INTL, Model Number DTBA2D4 recall — FDA Z-1737-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF CRT-D DTBB2Q1 VIVA QUAD S IS4/DF1 INTL, Model Number DTBB2Q1 recall — FDA Z-1747-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF CRTD DTPA2D1G COBALT XT HF QUAD OUS, Model Number DTPA2D1G recall — FDA Z-1775-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF ICD COBALT VR MRI IS1 DF1, Model Number DVPB3D1 recall — FDA Z-1820-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF ICD-DR DDMB1D4 EVERA MRI XT IS-1/DF4 US, Model Number DDMB1D4 recall — FDA Z-1712-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
Wilson-Cook Medical Hemospray Endoscopic Hemostat: Reference Part Numbers: a) HEMO-7, REF recall — FDA Z-1978-2023
There are potential risks of the Hemospray powder adhering to the distal end of the endoscope, which can result in adhesion of the endoscope to tissue and consequent difficulty or inability…
Class IIFDA: OngoingWilson-Cook Medical Inc.
Medical DeviceJun 28, 2023
CRHF ICD-VR DVAB1D4 VISIA AF US DF4, Model Number DVAB1D4 recall — FDA Z-1790-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF CRTD CROME HF QUAD MRI IS4 DF4, Model Number DTPC2QQ recall — FDA Z-1788-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF ICD-VR DVAB1D1 VISIA AF US IS1/DF1, Model Number DVAB1D1 recall — FDA Z-1789-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF CRT-D DTBC2Q1 BRAVA QUAD IS4/DF1 INTL, Model Number DTBC2Q1 recall — FDA Z-1751-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF ICD COBALT XT VR MRI DF4, Model Number DVPA2D4 recall — FDA Z-1819-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories